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ganciclovir sodium

NDC 70436-231, ganciclovir sodium, injection, powder, lyophilized, for solution, from Slate Run Pharmaceuticals, LLC.

Product NDC
70436-231
Status
Listed
Labeler
Slate Run Pharmaceuticals, LLC
Dosage form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204204
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70436-231 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • GANCICLOVIR SODIUM500 mg/10mL

Pharmacologic classes

Cytomegalovirus Nucleoside Analog DNA Polymerase Inhibitor [EPC]; DNA Polymerase Inhibitors [MoA]; Nucleoside Analog Antiviral [EPC]; Nucleoside Analog [EXT]

Package NDCNDC-11Package
70436-231-557043602315525 VIAL in 1 CARTON (70436-231-55) / 10 mL in 1 VIAL

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/cd293b9d-b573-4656-8574-19d7db870a9b

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=70436-231

Use it

Look up 70436-231 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70436-231 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70436-231. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.